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Journal Abstract Search

200 related items for PubMed ID: 35410579

  • 1.
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  • 2. Mutational screening of germline RB1 gene in Vietnamese patients with retinoblastoma reveals three novel mutations.
    Nguyen HH, Nguyen HTT, Vu NP, Le QT, Pham CM, Huyen TT, Manh H, Pham HLB, Nguyen TD, Le HTT, Van Nong H.
    Mol Vis; 2018; 24():231-238. PubMed ID: 29568217
    [Abstract] [Full Text] [Related]

  • 3. Spectrum of germline RB1 mutations and clinical manifestations in retinoblastoma patients from Thailand.
    Rojanaporn D, Boontawon T, Chareonsirisuthigul T, Thanapanpanich O, Attaseth T, Saengwimol D, Anurathapan U, Sujirakul T, Kaewkhaw R, Hongeng S.
    Mol Vis; 2018; 24():778-788. PubMed ID: 30636860
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  • 4. RB1 germline mutation spectrum and clinical features in patients with unilateral retinoblastomas.
    Fang X, Chen J, Wang Y, Zhao M, Zhang X, Yang L, Ni X, Zhao J, Gallie BL.
    Ophthalmic Genet; 2021 Oct; 42(5):593-599. PubMed ID: 34190019
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  • 6. Clinical characteristics and germline mutation spectrum of RB1 in Chinese patients with retinoblastoma: A dual-center study of 145 patients.
    Chai P, Luo Y, Yu J, Li Y, Yang J, Zhuang A, Fan J, Han M, Jia R.
    Exp Eye Res; 2021 Apr; 205():108456. PubMed ID: 33493472
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  • 7. Spectrum of germline mutations in RB1 in Chinese patients with retinoblastoma: Application of targeted next-generation sequencing.
    Zou Y, Li J, Hua P, Liang T, Ji X, Zhao P.
    Mol Vis; 2021 Apr; 27():1-16. PubMed ID: 33456302
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  • 10. A novel de-novo RB1 mutation identified in a patient with bilateral retinoblastoma.
    Fukushima H, Suzuki R, Hiraoka T, Suzuki S, Noguchi E, Takada H.
    Jpn J Clin Oncol; 2023 Aug 30; 53(9):863-865. PubMed ID: 37345682
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  • 13. Prenatal genetic diagnosis of retinoblastoma and report of RB1 gene mutation from India.
    Shah PK, Sripriya S, Narendran V, Pandian AJ.
    Ophthalmic Genet; 2016 Dec 30; 37(4):430-433. PubMed ID: 26914665
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  • 14. Association Between Genotype and Phenotype in Consecutive Unrelated Individuals With Retinoblastoma.
    Salviat F, Gauthier-Villars M, Carton M, Cassoux N, Lumbroso-Le Rouic L, Dehainault C, Levy C, Golmard L, Aerts I, Doz F, Bonnet-Serrano F, Hayek S, Savignoni A, Stoppa-Lyonnet D, Houdayer C.
    JAMA Ophthalmol; 2020 Aug 01; 138(8):843-850. PubMed ID: 32556071
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  • 15. Osteosarcoma without prior retinoblastoma related to RB1 low-penetrance germline pathogenic variants: A novel type of RB1-related hereditary predisposition syndrome?
    Imbert-Bouteille M, Gauthier-Villars M, Leroux D, Meunier I, Aerts I, Lumbroso-Le Rouic L, Lejeune S, Delnatte C, Abadie C, Pujol P, Houdayer C, Corsini C.
    Mol Genet Genomic Med; 2019 Dec 01; 7(12):e913. PubMed ID: 31568710
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  • 16. RB1 gene mutations and genetic spectrum in retinoblastoma cases.
    Akdeniz Odemis D, Kebudi R, Bayramova J, Kilic Erciyas S, Kuru Turkcan G, Tuncer SB, Sukruoglu Erdogan O, Celik B, Kurt Gultaslar B, Buyukkapu Bay S, Tuncer S, Yazici H.
    Medicine (Baltimore); 2023 Sep 08; 102(36):e35068. PubMed ID: 37682130
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  • 17. A novel deep intronic low penetrance RB1 variant in a retinoblastoma family.
    Soliman SE, Racher H, Lambourne M, Matevski D, MacDonald H, Gallie B.
    Ophthalmic Genet; 2018 Apr 08; 39(2):288-290. PubMed ID: 29099630
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  • 18. Identification of novel RB1 genetic variants in Retinoblastoma patients and their impact on clinical outcome.
    Manukonda R, Pujar A, Ramappa G, Vemuganti GK, Kaliki S.
    Ophthalmic Genet; 2022 Feb 08; 43(1):64-72. PubMed ID: 34645364
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  • 20. Simultaneous identification of clinically relevant RB1 mutations and copy number alterations in aqueous humor of retinoblastoma eyes.
    Xu L, Shen L, Polski A, Prabakar RK, Shah R, Jubran R, Kim JW, Biegel J, Kuhn P, Cobrinik D, Hicks J, Gai X, Berry JL.
    Ophthalmic Genet; 2020 Dec 08; 41(6):526-532. PubMed ID: 32799607
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